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The Vanderbilt Urologic Infection Repository, a Resource for Personalized Clinical Discovery

The Vanderbilt Urologic Infection Repository, a Resource for Personalized Clinical Discovery
范德比尔特泌尿感染存储库,个性化临床发现的资源
批准号:
10022306
负责人:
Maria Hadjifrangiskou
金额:
$25.24万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
已结题
起止时间:
至 2022-06-30
关键词:
Acinetobacter baumanniiAgeAnatomyAntibiotic susceptibilityBacteremiaBacteriuriaBioinformaticsBiologicalCLIA certifiedCaringCatalogsCategoriesCathetersClinicalClinical DataClinical MicrobiologyCollectionCommunicable DiseasesCommunitiesCystitisDataDatabasesDiagnosticElectronic Health RecordEquilibriumEscherichia coliEthicsFoundationsGenesGeneticGenetic PolymorphismGenitourinary systemGenomicsGenotypeGenus staphylococcusGestational DiabetesHealthHeterogeneityHumanIndividualInfectionInformaticsInfrastructureInstitutionKnowledgeLaboratoriesLightLinkLogisticsMachine LearningMedicalMedical InformaticsMedical centerMethodsMicrobial Genome SequencingMicrobiologyMiningModelingMolecularOrganismPathogenesisPathologyPatient CarePatientsPhenotypePhysiciansPilot ProjectsPrecision Medicine InitiativeProtocols documentationPublic DomainsPyelonephritisReportingResearchResearch PersonnelResource InformaticsResourcesRisk FactorsSiteSourceSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationSterilityTaxonomyTechnologyTherapeuticUncertaintyUrinary tract infectionUrineUrologyUropathogenbasebiobankclinical encounterclinical practiceclinical sequencingclinically actionableclinically relevantcombatdemographicsevidence basegenome sequencinggenome wide association studygenomic datahigh throughput technologyinterestmicrobialmicrobial genomemicrobial genomicspathogenpathogen genomepatient health informationphenomephenotypic dataprognostic toolprogramsprotein profilingrepositorysexsymptomatologytooltranslational impacturologicwhole genomeyoung woman

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中文摘要
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英文摘要
SUMMARY - RESOURCE PROJECT Urinary tract infections (UTIs) represent not only one of the most prevalent urologic pathologies, but also one of the most diverse. With both traditional and emerging risk factors, commonly encountered clinical scenarios range from asymptomatic bacteriuria and uncomplicated cystitis to pyelonephritis, bacteremia, and outright urosepsis. The causative microbial agents likewise include a tremendous variety of opportunistic pathogens, with additional (and significant) genotypic/phenotypic diversity among individual strains of these species. On a molecular level, the host-pathogen factors that dictate the balance between urologic health and UTI remain incompletely defined. Generalized models of pathogenesis fail to account for commonly encountered nuances of real-world clinical practice, limiting the ability of physicians to provide care that is both evidence-based and personalized. To combat these challenges, we seek to create the Vanderbilt Urologic Infection Repository (VUIR): a massive (but de-identified) collection of patient-specific clinical information and paired microbial isolates, repurposed from our Medical Center's routine workflow of diagnostic urine cultures. As both an informatic and biologic resource, the VUIR will build on unique foundations that are already in place at Vanderbilt. These include our Synthetic Derivative, an anonymized mirror of our electronic health records, along with microVU, an initiative through which all sterile-site microbial isolates from our Diagnostic Laboratories are systematically retained for academic inquiry. We now propose to expand microVU activities to include Vanderbilt's formidable volume of urine cultures, linking the banked organisms (many thousand annually) to key searchable parameters from the source-patients (e.g. demographics, symptomatology, risk factors), as well as the broader body of data within the Synthetic Derivative. As a two-way bridge, the VUIR will create an opportunity to parse human phenomes in light of microbiologic results, while providing a tremendous quantity of wild-type microbial strains for downstream experimentation, all stratified by human UTI-phenotypes. One particularly exciting application of the VUIR involves genome-wide association studies (GWAS) that network genetic features of pathogens directly to clinical features of their hosts. In addition to building the VUIR, we will mine the repository to select underrepresented microbial targets for whole-genome sequencing. Through a machine-learning approach, the multi-partite genomic features of these strains will be correlated to their hosts' clinical parameters, with an emphasis on Escherichia coli and the global phenotypes of [1] symptomatic UTI and [2] asymptomatic bacteriuria (ASB). The microbial features that distinguish these phenomenological categories remain poorly defined—at least by the simplified metrics considered to date—although a rigorous molecular definition of UTI- vs-ASB would carry significant diagnostic value for physicians and pathogenetic value for investigators. In light of this complexity, we will utilize the VUIR to harmonize bioinformatic and medical informatic data across host and pathogen, as proof-of-concept for this program's broad utility in clinical/basic urology and allied fields.
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会议论文
Targeting cytochrome bd as an anti-biofilm strategy
How E. coli Acid Response Mechanisms Breach Colonization Resistance in the Vagina
Two-component system interactions as uropathogenic Escherichia coli drug targets
  • 批准号:
    8816807
  • 项目类别:
  • 资助金额:
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  • 财政年份:
    2014
  • 负责人:
    Maria Hadjifrangiskou
  • 依托单位:
Two-component system interactions as uropathogenic Escherichia coli drug targets
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